We present a numerical study of the doping dependence of the spectral
function of the n-type cuprates. Using a variational cluster-perturbation
theory approach based upon the self-energy-functional theory, the spectral
function of the electron-doped two-dimensional Hubbard model is calculated. The
model includes the next-nearest neighbor electronic hopping amplitude t′ and
a fixed on-site interaction U=8t at half filling and doping levels ranging
from x=0.077 to x=0.20. Our results support the fact that a comprehensive
description of the single-particle spectrum of electron-doped cuprates requires
a proper treatment of strong electronic correlations. In contrast to previous
weak-coupling approaches, we obtain a consistent description of the ARPES
experiments without the need to introduce a doping-dependent on-site
interaction U.Comment: 7 pages 4 eps figure